FDA Inspection 582805 — Cochlear Americas Inc.

Cochlear Americas Inc. — FEI 3005900820

The FDA completed an inspection of Cochlear Americas Inc. on May 12, 2009 in Lone Tree, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 12, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lone Tree, CO (United States)

Additional Details

Sponsor, Contract Research Organization